ID: 132090766 | Neanderthal introgressed variant-containing enhancer experimental_89387 [Homo sapiens (human)] | Chromosome 6, NC_000006.12 (121467118..121467287) | | |
ID: 132089330 | Neanderthal introgressed variant-containing enhancer experimental_89339 [Homo sapiens (human)] | Chromosome 6, NC_000006.12 (121428959..121429128) | | |
ID: 127407154 | H3K4me1 hESC enhancer GRCh37_chr6:121768815-121769315 [Homo sapiens (human)] | Chromosome 6, NC_000006.12 (121447669..121448169) | | |
ID: 127407153 | H3K4me1 hESC enhancer GRCh37_chr6:121768314-121768814 [Homo sapiens (human)] | Chromosome 6, NC_000006.12 (121447168..121447668) | | |
ID: 127407152 | OCT4-NANOG-H3K27ac-H3K4me1 hESC enhancer GRCh37_chr6:121759052-121759929 [Homo sapiens (human)] | Chromosome 6, NC_000006.12 (121437906..121438783) | | |
ID: 127407151 | OCT4-NANOG-H3K27ac-H3K4me1 hESC enhancer GRCh37_chr6:121751780-121752762 [Homo sapiens (human)] | Chromosome 6, NC_000006.12 (121430634..121431616) | | |
ID: 124901515 | uncharacterized LOC124901515 [Homo sapiens (human)] | Chromosome 6, NC_000006.12 (121443617..121443693) | | |
ID: 106481182 | RNA, U4 small nuclear 35, pseudogene [Homo sapiens (human)] | Chromosome 6, NC_000006.12 (121453981..121454121, complement) | | |
ID: 100874472 | high mobility group nucleosomal binding domain 2 pseudogene 29 [Homo sapiens (human)] | Chromosome 6, NC_000006.12 (121408411..121409015) | | |
ID: 100271357 | ribosomal protein S15a pseudogene 21 [Homo sapiens (human)] | Chromosome 6, NC_000006.12 (121381439..121381896) | RPS15A_6_747 | |
ID: 260339 | transcription factor A, mitochondrial pseudogene [Homo sapiens (human)] | Chromosome 6, NC_000006.12 (121478167..121479288, complement) | | |
ID: 2697 | gap junction protein alpha 1 [Homo sapiens (human)] | Chromosome 6, NC_000006.12 (121435646..121449727) | AVSD3, CMDR, CX43, EKVP, EKVP3, GJAL, HLHS1, HSS, ODDD, PPKCA | 121014 |